{{Rsnum
|rsid=569688
|Chromosome=8
|position=60049262
|Orientation=minus
|GMAF=0.2612
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 3.5 | 31.0 | 65.5
| HCB | 12.4 | 45.3 | 42.3
| JPT | 10.6 | 45.1 | 44.2
| YRI | 1.4 | 15.6 | 83.0
| ASW | 1.8 | 21.1 | 77.2
| CHB | 12.4 | 45.3 | 42.3
| CHD | 11.0 | 44.0 | 45.0
| GIH | 3.0 | 18.8 | 78.2
| LWK | 0.0 | 17.3 | 82.7
| MEX | 29.3 | 50.0 | 20.7
| MKK | 1.3 | 33.3 | 65.4
| TSI | 5.9 | 30.4 | 63.7
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23049088
  |Trait=Myopia (pathological)
  |Title=A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population.
  |RiskAllele=
  |Pval=4E-7
  |OR=NR
  |ORtxt=NR
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}